Clinical Research Coordinator II: Lead Multi-Trial Studies

Velocity-Clinical-Research,-Inc.

Maplewood (MO)

On-site

USD 52,000 - 66,000

Full time

11 days ago
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Job summary

Velocity Clinical Research is seeking a Clinical Research Coordinator II to manage multiple trials from start-up to close-out in compliance with protocol, GCP and Velocity SOPs. You will coordinate start-up activities, site qualification, regulatory documents and subject scheduling, while safeguarding data quality and patient safety.

Ideal candidates have a Bachelor’s degree with life science experience or equivalent, strong organizational and communication skills, and the ability to work in a

Qualifications

  • Bachelor’s degree with 2 years life science experience
  • Associate’s degree with 4 years life science experience
  • High School diploma with 6 years life science experience and 1 year Clinical Research Coordinator experience

Responsibilities

  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
  • Coordinate start up, vendor management, subject recruitment, source development review, scheduling visits, and regulatory documents
  • Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study
  • Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols
  • Communicate effectively with coworkers, leadership, sponsors, CROs, and vendors
  • Apply good documentation practices when collecting data, transferring data to sponsor/CRO data capture systems and resolving queries
  • Maintain confidentiality of patient information and Velocity confidential information
  • Verify and elevate patient safety concerns by ensuring adverse events are followed and reported
  • Ensure data entry into sponsor data portal and timely query resolution
  • Ensure staff are trained and delegated appropriately
  • Create, collect and submit regulatory documents to Sponsors and IRBs as required

Skills

Medical terminology
Microsoft Office
Communication skills
Organizational skills
Team player
English proficiency
Multi-tasking
Detail oriented
Problem solving
Leadership
Adaptability

Education

Bachelor’s degree with life science experience
Associate’s degree with life science experience
High School diploma with life science experience + CRC experience

Job description

Velocity Clinical Research is seeking a Clinical Research Coordinator II to manage multiple trials from start-up to close-out in compliance with protocol, GCP and Velocity SOPs. You will coordinate start-up activities, site qualification, regulatory documents and subject scheduling, while safeguarding data quality and patient safety.

Ideal candidates have a Bachelor’s degree with life science experience or equivalent, strong organizational and communication skills, and the ability to work in a

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